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SUMMARY
- INLEXZO (gemcitabine intravesical system) is an intravesical drug releasing system (iDRS), referred to as TAR-200 in literature.1
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- Daneshmand et al (2024)2 presented results of Project Penelope, a preclinical study that compared the penetration, retention, and tissue distribution of gemcitabine and its active metabolites (diphosphate and triphosphate of gemcitabine) with INLEXZO vs traditional intravesical instillation methods in minipigs (N=5).
PRECLINICAL DATA
Project Penelope
Daneshmand et al (2024)2 compared the penetration, retention, and tissue distribution of gemcitabine and its active metabolites (diphosphate and triphosphate of gemcitabine) with INLEXZO vs traditional intravesical instillation methods in minipigs (N=5).
Study Design/Methods
- Three minipigs were treated with intravesical gemcitabine instillation, and 2 minipigs were treated with INLEXZO.
- All minipigs were assessed for penetration of active gemcitabine metabolites across different tissues of the bladder wall for over 96 hours.
- Collected samples included the dome (urothelium and lamina propria), left and right lateral wall, and trigone. Processed samples were analyzed for gemcitabine and its active metabolites using liquid chromatography tandem mass spectrometry (LC-MS/MS).
- The 3 minipigs receiving intravesical gemcitabine instillation were administered a 50 mL solution containing 2 g of freebase equivalent of gemcitabine hydrochloride (dissolved in saline at 40 mg/mL) via a Foley balloon catheter for 2 hours.
- The 2 minipigs receiving INLEXZO were administered 225 mg of freebase equivalent of gemcitabine. INLEXZO was inserted directly into the bladder, which was left in place for the duration of the study until necropsy.
- Tissue samples were collected at necropsy at different time intervals after instillation (animal 1, 2 hours; animal 6, 24 hours; animal 5, 96 hours) and INLEXZO insertion (animal 4, 48 hours; animal 3, 96 hours), respectively. See Figure: Treatment Administration Schedule for Minipigs.
Treatment Administration Schedule for Minipigs2

Results
Intravesical Gemcitabine Instillation
Mean Concentrations of Gemcitabine Active Metabolites in Bladder Tissue Layers After Intravesical Gemcitabine Instillation2

Abbreviations: dFdCDP, diphosphate of gemcitabine; dFdCTP, triphosphate of gemcitabine; Instill, instillation; LP, lamina propria; Uro, urothelium.
Notes: Results were reported as the mean of the 4 tissue samples collected (dome, left and right lateral wall, and trigone). Results from the total tissue sample or by tissue type (urothelium/lamina propria and muscle wall) are reported separately. All refers to all layers of the bladder. Gemcitabine active metabolites defined as diphosphate and triphosphate of gemcitabine.
INLEXZO
- With INLEXZO treatment, gemcitabine diphosphate and triphosphate levels were detectable in all bladder tissue layers during the 48 hours and 96 hours indwelling period; see Figure: Mean Concentrations of Gemcitabine Active Metabolites in Bladder Tissue Layers After Treatment With INLEXZO.
- Active metabolite concentrations were higher in the urothelium and lamina propria than in the muscle and remained for up to 96 hours in both tissue samples.
- Active metabolite concentrations were lower than those observed 2 hours after gemcitabine instillation but were sustained across all bladder tissues for up to 96 hours.
Mean Concentrations of Gemcitabine Active Metabolites in Bladder Tissue Layers After Treatment With INLEXZO2

Abbreviations: dFdCDP, diphosphate of gemcitabine; dFdCTP, triphosphate of gemcitabine; LP, lamina propria; Uro, urothelium.
Notes: Results were reported as the mean of the 4 tissue samples collected (dome, left and right lateral wall, and trigone). Results from the total tissue sample or by tissue type (urothelium/lamina propria and muscle wall) are reported separately. All refers to all layers of the bladder. Gemcitabine active metabolites defined as diphosphate and triphosphate of gemcitabine.
LiTerature Search
A literature search of MEDLINE®, Embase®, BIOSIS Previews®, and Derwent Drug File (and/or other resources, including internal/external databases) was conducted on 20 November 2025.
| 1 | Daneshmand S, Van der Heijden MS, Jacob JM, et al. TAR-200 for Bacillus Calmette-Guérin-unresponsive high-risk non-muscle-invasive bladder cancer: results from the phase IIb SunRISe-1 study. J Clin Oncol. 2025;43(33):3578-3588. |
| 2 | Daneshmand S, Wuyts K, Meulder MD, et al. Penelope: tissue penetration of gemcitabine phosphate metabolites following TAR-200 administration vs standard intravesical instillation in minipigs. Poster presented at: Society of Urologic Oncology (SUO) Annual Meeting; December 4-6, 2024; Dallas, TX. |